ZnO/reduced graphene oxide/polypyrrole ternary composite material preparation method, and application of the ternary composite material
A composite material and ternary composite technology, applied in electrical components, hybrid capacitor electrodes, electrolytic capacitors, etc., can solve the problems of poor capacity ratio and stability, poor cycle performance, low specific capacitance, etc., and achieve enhanced capacitance performance, The effect of low cost and high energy density
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Embodiment 1
[0039] (1) Preparation of GO
[0040] a. Take 92mL of concentrated sulfuric acid and place it in an ice-water bath, lower the temperature to 0-5°C, slowly add 4g of natural graphite and 2g of anhydrous sodium nitrate, and continue stirring for 30min.
[0041] b. Add 13 g of potassium permanganate to the above mixed solution, maintain the ice bath for 1 h, take the mixed solution out of the ice bath, stir at room temperature for 3 h, and add 180 mL of water dropwise, and stir for 20 min.
[0042] c. Continue to add 560mL water to the mixed solution, and then add 50mL 30% hydrogen peroxide drop by drop. When the supernatant is colorless, remove the supernatant, then add 560mL water, adjust the pH to 7 with KOH, and remove the supernatant after standing still for 24 hours The solution was filtered with a circulating water vacuum pump, soaked in ethanol, washed with water, and dried in vacuum at 60°C for 24 hours to obtain GO.
[0043] (2) Preparation of ZnO / RGO binary composites...
Embodiment 2
[0055] (1) Preparation of GO: Same as Example 1.
[0056] (2) Preparation of ZnO / RGO binary composite: Same as Example 1.
[0057] (3) Synthesis of ZnO / RGO / PPy ternary composites
[0058] a. Disperse 0.1077g ZnO / RGO into 100mL aqueous solution dissolved with 0.5g cetyltrimethylammonium bromide (CTAB) and sonicate for 2h.
[0059] b. The above dispersion was taken out and placed in an ice-water bath and kept stirring. At the same time, 20 mL of ethanol solution in which 14.4 mmol of Py monomer was dissolved was slowly added and ultrasonicated for 30 min to completely adsorb Py on the ZnO / RGO composite.
[0060] c. Slowly add 30 mL of 14.4 mmol (NH 4 ) 2 S 2 o 8 The aqueous solution was stirred and reacted in an ice bath for 24 hours, filtered, washed, and dried at 60°C to obtain the ZnO / RGO / PPy ternary composite material (A). Among them: the mass ratio of ZnO / RGO to Py monomer is 1:9.
[0061] (4) Fabrication of ZnO / RGO / PPy ternary composite electrodes
[0062] a. Mix t...
Embodiment 3
[0068] (1) Preparation of GO: Same as Example 1.
[0069] (2) Preparation of ZnO / RGO binary composite: Same as Example 1.
[0070] (3) Synthesis of ZnO / RGO / PPy ternary composites
[0071] a. Disperse 0.1038g ZnO / RGO into 100mL aqueous solution dissolved with 0.5g cetyltrimethylammonium bromide (CTAB) and sonicate for 2h.
[0072] b. The above dispersion was taken out and placed in an ice-water bath and kept stirring. At the same time, 20 mL of ethanol solution in which 3.6 mmol of Py monomer was dissolved was slowly added and ultrasonicated for 30 min to completely adsorb Py on the ZnO / RGO composite.
[0073] c. Slowly add 30 mL of 3.6 mmol (NH 4 ) 2 S 2 o 8 Aqueous solution of ZnO / RGO / PPy ternary complex (B) was obtained by stirring in an ice bath for 24 hours, filtering, washing, and drying at 60°C. Among them: the mass ratio of ZnO / RGO to Py monomer is 3:7.
[0074] (4) Fabrication of ZnO / RGO / PPy ternary composite electrode: the method is the same as in Example 2.
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